ZipRecruiter

Log In

1

Clinical Study Jobs (NOW HIRING)

Axogen

Clinical Study Manager

Tampa, FL · On-site

Job Summary of the Clinical Study Manager The Clinical Study Manager (CSM) is accountable for the end-to-end operational leadership of an Axogen-sponsored randomized controlled trial (RCT) and other ...

Danaher

Senior Clinical Study Manager

The Senior Clinical Study Manager is responsible for clinical trial execution within the US and EU regions for Leica Biosystems. This role will specifically support Leica Biosystems, an operating ...

Mobia Medical, Inc.

Clinical Study Manager

Fridley, MN · On-site

$110K - $160K/yr

About the role The Clinical Study Manager is a key member of the Clinical Affairs team, responsible for leading the operational execution and management of clinical studies that support the company ...

Danaher

Senior Clinical Study Manager

OR · Remote

The Senior Clinical Study Manager is responsible for clinical trial execution within the US and EU regions for Leica Biosystems. This role will specifically support Leica Biosystems, an operating ...

Spyglass Pharma

Clinical Study Manager

Aliso Viejo, CA · On-site

$140K - $160K/yr

Summary: The Clinical Study Manager (CSM) plays a key role in the planning and execution of SpyGlass Pharma's clinical trials. Working closely with the Director of Clinical Research and cross ...

Axogen

Clinical Study Manager

Tampa, FL

Job Summary of the Clinical Study Manager The Clinical Study Manager (CSM) is accountable for the end‑to‑end operational leadership of an Axogen‑sponsored randomized controlled trial (RCT) and ...

Icon plc

Clinical Study Specialist

Basking Ridge, NJ · Hybrid

Clinical Study Specialist ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven ...

Icon plc

Clinical Study Specialist

Cambridge, MA · Hybrid

Clinical Study Specialist ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven ...

Danaher

Senior Clinical Study Manager

Chaska, MN · On-site

$135K/yr

The Senior Clinical Study Manager is responsible for managing clinical trial execution from feasibility assessments through study closeout. This position reports to the Senior Manager Clinical ...

New

Penumbra

Clinical Study Manager

General Summary The Clinical Study Manager provides leadership in the planning, design, and execution of clinical studies sponsored by Penumbra to assess safety and effectiveness of products. This ...

Propedix, Inc.

Clinical Study Coordinator

Milford, MA

$25 - $30/hr

Clinical Study Coordinator (Consultant) About the Company: Propedix is a biopharma and consumer health company dedicated to advancing innovative treatments in healthcare. Our flagship product ...

next page

Showing results 1-20

People also search for

All JobsClinical Study Jobs

Clinical Study information

See salary details

$22K

$125.3K

$206K

How much do clinical study jobs pay per year?

As of Jun 5, 2026, the average yearly pay for clinical study in the United States is $125,290.00, according to ZipRecruiter salary data. Most workers in this role earn between $85,000.00 and $157,000.00 per year, depending on experience, location, and employer.

What are clinical studies?

Clinical studies are research investigations conducted with human volunteers to evaluate the safety, effectiveness, and side effects of medical treatments, drugs, devices, or interventions. These studies follow strict scientific and ethical guidelines and are usually carried out in several phases before a treatment can be approved for widespread use. Clinical studies help determine whether new approaches to prevention, diagnosis, or therapy are safe and effective for people. Participation in clinical studies is voluntary and can contribute to advancements in medical science.

What job pays 400,000 a year without a degree?

In the field of clinical studies, high-paying roles such as clinical research managers or directors can reach salaries around $400,000 annually, especially with extensive experience and leadership responsibilities. These positions often require strong project management skills, industry knowledge, and certifications like RAC or CCR, but may not always require a traditional degree if complemented by significant experience and expertise.

What are some common challenges faced when managing multiple clinical studies simultaneously?

Professionals involved in clinical studies often juggle several projects at once, which can present challenges such as balancing competing timelines, ensuring regulatory compliance across studies, and coordinating with diverse teams. Effective project management, clear communication, and strong organizational skills are key to addressing these challenges. Utilizing project management tools and maintaining detailed documentation can help keep studies on track and reduce the risk of errors or delays.

What is the difference between Clinical Study vs Clinical Research Coordinator?

AspectClinical StudyClinical Research Coordinator
CredentialsOften requires a degree in health sciences, nursing, or related fields; certifications like CCRP are commonTypically holds a bachelor's degree in health sciences, nursing, or related fields; certifications like CCRP or CRC are advantageous
Work EnvironmentConducted in hospitals, clinics, or research facilities; involves direct patient interaction and data collectionWorks in research sites, hospitals, or clinics; manages study logistics and coordinates between teams
Employer & IndustryPharmaceutical companies, academic institutions, CROsResearch institutions, hospitals, pharmaceutical companies

While both roles are integral to clinical research, a Clinical Study typically refers to the overall research process or specific studies, whereas a Clinical Research Coordinator is a professional who manages and oversees the day-to-day operations of clinical trials. Understanding these distinctions helps in choosing the right career path or job search focus.

What are the key skills and qualifications needed to thrive as a Clinical Study Coordinator, and why are they important?

To thrive as a Clinical Study Coordinator, you need a solid understanding of clinical research protocols, regulatory guidelines like GCP, and often a degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and sometimes certification such as CCRC or CCRA is typically required. Strong organizational skills, attention to detail, and effective communication are crucial soft skills for coordinating multiple tasks and interacting with diverse stakeholders. These skills ensure compliance, accurate data collection, and smooth trial operations, which are vital for the integrity and success of clinical studies.
More about Clinical Study jobs
What cities are hiring for Clinical Study jobs? Cities with the most Clinical Study job openings:
What are the most commonly searched types of Clinical Study jobs? The most popular types of Clinical Study jobs are:
What states have the most Clinical Study jobs? States with the most job openings for Clinical Study jobs include:
Clinical Study jobs near you
Infographic showing various Clinical Study job openings in the United States as of May 2026, with employment types broken down into 3% Locum Tenens, 47% Full Time, 13% Part Time, and 37% Contract. Highlights an 83% Physical, 3% Hybrid, and 14% Remote job distribution, with an average salary of $125,290 per year, or $60.2 per hour.
Clinical Study Manager

Clinical Study Manager

Axogen

Tampa, FL • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 27 days ago

Job description

Axogen is committed to building and maintaining a strong and gratifying company culture that fosters professional growth. Our hands-on and personal approach makes transitioning to a new job a seamless and enjoyable process. Most benefits are effective on day one!
Axogen is an equal opportunity employer and does not discriminate against applicants on the basis of race, color, creed, religion, ancestry, age, sex, marital status, national origin, disability or veteran status.
Why you'll love working at Axogen:
  • Friendly, open, and fun team culture that values unique perspectives
  • Company-wide dedication to profoundly impacting patients' lives
  • Comprehensive, high-quality benefits package effective on date of hire
  • Educational assistance available for all employees
  • Matching 401(k) retirement plan
  • Paid holidays, including floating holidays, to be used at your discretion
  • Employee Stock Purchase Plan
  • Referral incentive program

Axogen Mission and Business Purpose
Our business purpose is to restore health and improve quality of life by making restoration of peripheral nerve function an expected standard of care. We aim to lead the markets we serve by always requiring the solutions we offer patients and caregivers provide an improved benefit-to-risk profile as compared to existing standards of care. To ensure we deliver improved benefit-to-risk solutions, we will guide and expect the market and design requirement specifications underlying our engineering, business development, and clinical research activities, objectively target advancements in standards of care.
Job Summary of the Clinical Study Manager
The Clinical Study Manager (CSM) is accountable for the end-to-end operational leadership of an Axogen-sponsored randomized controlled trial (RCT) and other complex prospective clinical studies conducted in highly regulated environments, including biologics, combination products, and medical devices. This role is intended for a highly experienced clinical operations professional who can independently own study execution, serve as the operational authority for an assigned trial, and act as a role model for CRAs, vendors, and cross-functional partners. The CSM is responsible for ensuring exceptional execution quality, data integrity, and inspection readiness while maintaining the highest standards of ethics and Good Clinical Practice (GCP).
Requirements of the Clinical Study Manager
  • Bachelor's degree or higher in a scientific, medical, or engineering discipline (or equivalent experience).
  • Minimum 5 years of industry-sponsored clinical research experience.
  • Demonstrated experience leading complex prospective interventional studies, with RCT experience strongly preferred.
  • Experience conducting studies in biologics, combination products, and/or medical devices.
  • Proven track record of maintaining high data integrity, compliance, and inspection readiness.
  • Strong working knowledge of ICH-GCP and global regulatory requirements.
  • Willingness and ability to travel up to 50%.

Responsibilities of the Clinical Study Manager
The specific duties of the Clinical Study Manager include but are not limited to:
Clinical Operations Leadership
  • Lead the planning, start-up, execution, monitoring, and close out of large, complex prospective clinical studies, including RCTs.
  • Serve as the study level operational owner, accountable for timelines, quality, compliance, and execution excellence.
  • Translate protocol intent and regulatory requirements into robust, executable clinical operations strategies.

Study Planning & Execution
  • Develop and execute comprehensive:
    • Clinical Operations Plans
    • Monitoring Plans
    • Vendor Oversight Plans
    • Recruitment and retention strategies
    • Study timelines, budgets, and resourcing plans
    • Ensure study conduct aligns with protocol, SAP, investigational plan, and regulatory commitments.

Quality, Compliance, and Inspection Readiness
  • Ensure continuous compliance with:
    • ICH-GCP
    • FDA and OUS regulatory requirements
    • Internal SOPs and quality standards
  • Proactively identify and mitigate risks to subject safety, data integrity, and regulatory compliance.
  • Lead and support audit and inspection readiness, responses, and CAPA development.

Vendor & Site Oversight
  • Lead selection, onboarding, and oversight of CROs and other clinical vendors.
  • Drive vendor performance through KPIs, issue escalation, and corrective actions.
  • Oversee site selection, activation, and ongoing performance, including the performance of on-site visits, enrollment tracking, monitoring quality, protocol adherence.

Team Leadership & Mentorship
  • Provide leadership, mentoring, and professional guidance to CRAs and study team members.
  • Serve as a role model for best-in-class clinical operations conduct, documentation quality, and ethical decision-
  • Contribute to SOPs, work instructions, templates, and training materials.

Location
111 West Oak Ave., Tampa, FL 33602
#LI-AC1
Benefits/Compensation
This position is eligible for an annual bonus.
Benefits offered for this position include Health, Dental, Vision, Matching 401K, Paid Time Off, 9 Paid Holidays + 3 Floating Holidays, Dependent Care Flexible Spending Accounts, Medical Flexible Spending Accounts, Tuition Reimbursement, Paid Parental Leave, Paid Caregiver Leave, Basic Life Insurance, Supplemental Life Insurance, Employee Stock Purchase Plan, and Disability Insurance, as described in more detail in summary plan descriptions.
Salary Range
$113,903-$142,378 USD
Axogen follows healthcare system guidelines with respect to credentialing, vaccinations and other employment/compliance related requirements, as well as CDC guidance. Axogen reserves the right to amend its policies from time to time in its sole discretion.

Apply